| Autor: |
Walter Leonardo Alves Gusmão, Antônio Marcos da Silva Catharino, Jacqueline Stephanie Fernandes do Nascimento, Master Degree in neurology at Hugg Neurologist at Hgni, Nova Iguaçu Medical Student at Unig, Janie Kelly Fernandes do Nascimento, M Gilberto Canedo, Tatiane Daniele de Almeida Costa, Marco Antonio Orsini Neves, Nicolle dos Santos Moraes Nunes |
| Rok vydání: |
2020 |
| Předmět: |
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| Zdroj: |
The Gazette of Medical Sciences. 1:73-77 |
| ISSN: |
2692-4374 |
| DOI: |
10.46766/thegms.neuro.20102304 |
| Popis: |
Tuberous Sclerosis Complex or Bourneville’s disease is an autosomal dominant disease with high penetrance and variability characterized by multisystem involvement by benign lesions, originally defined by the classic triad of Vogt: sebaceous adenoma, epilepsy and mental retardation. The involvement of the brain is responsible for a significant proportion of the morbidity and mortality of this disease and skin lesions are the most common manifestations. The authors report 31-year-old patient case referred to the service by intractable epilepsy with definitive clinical criteria for tuberous sclerosis. |
| Databáze: |
OpenAIRE |
| Externí odkaz: |
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